NextSeq 500 paired end sequencing - SRA

ERX4753338: NextSeq 500 paired end sequencing
1 ILLUMINA (NextSeq 500) run: 654,711 spots, 104.8M bases, 40.4Mb downloads

Design: Paired-End Sequencing

Submitted by: EUROPEAN MOLECUALR BIOLOGY LABORATORY, GENOME BIOLOGY UNIT (EUROPEAN MOLECUALR BIOLOGY LABORATORY, GENOME BIOL)

Study: Strand-seq data of HGSVC samples

PRJEB39750 • ERP123307 • All experiments • All runs

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Strand-seq (single-cell and single-strand sequencing) libraries were generated for human lymphoblastic cell lines (LCL) to produce haplotype-informative data for select human genomes as part of the HGSVC (Human Genome Structural Variation Consortium) project - phase 2.

Sample: Coriell GM18534

SAMN00000419 • SRS000649 • All experiments • All runs

Organism: Homo sapiens

Library:

Name: GM18534_PE20384

Instrument: NextSeq 500

Strategy: WGS

Source: GENOMIC

Selection: MNase

Layout: PAIRED

Construction protocol: Strand-Seq

Runs: 1 run, 654,711 spots, 104.8M bases, 40.4Mb

Run	# of Spots	# of Bases	Size	Published
ERR4884401	654,711	104.8M	40.4Mb	2020-12-11

ID:: 12642306

SRA

Sequence Read Archive

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